LOC126805881[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155448	GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3	LOC129931453, LOC129931454 +1585 more	Copy number gain	See cases	GPathogenic
Select item 151159	GRCh38/hg38 1q21.3-23.1(chr1:154566501-157624084)x3	ADAM15, ADAM15-EFNA4 +297 more	Copy number gain	See cases	GPathogenic
Select item 1252028	NM_031282.3(FCRL4):c.847+1G>A	FCRL4, LOC126805881	Single nucleotide variant (splice donor variant)	not specified	GUncertain significance
Select item 2455642	NM_031282.3(FCRL4):c.823C>A (p.Pro275Thr)	FCRL4, LOC126805881 (P275T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278400	NM_031282.3(FCRL4):c.802G>A (p.Gly268Ser)	FCRL4, LOC126805881 (G268S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 783951	NM_031282.3(FCRL4):c.764A>G (p.Asn255Ser)	FCRL4, LOC126805881 (N255S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3094215	NM_031282.3(FCRL4):c.730C>G (p.Pro244Ala)	FCRL4, LOC126805881 (P244A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094214	NM_031282.3(FCRL4):c.649C>T (p.Pro217Ser)	FCRL4, LOC126805881 (P217S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411296	NM_031282.3(FCRL4):c.644A>G (p.Gln215Arg)	FCRL4, LOC126805881 (Q215R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410641	NM_031282.3(FCRL4):c.612G>T (p.Glu204Asp)	FCRL4, LOC126805881 (E204D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386927	NM_031282.3(FCRL4):c.533G>A (p.Arg178Lys)	FCRL4, LOC126805881 (R178K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2484379	NM_031282.3(FCRL4):c.526G>A (p.Val176Ile)	FCRL4, LOC126805881 (V176I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094213	NM_031282.3(FCRL4):c.427C>A (p.Leu143Ile)	FCRL4, LOC126805881 (L143I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2495172	NM_031282.3(FCRL4):c.357G>C (p.Leu119Phe)	FCRL4, LOC126805881 (L119F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance